首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Distribution and origin of the basement membrane component perlecan in rat liver and primary hepatocyte culture.
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Distribution and origin of the basement membrane component perlecan in rat liver and primary hepatocyte culture.

机译:大鼠肝和原代肝细胞培养物中基底膜成分perlecan的分布和来源。

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摘要

Basement membranes contain three major components (ie collagen IV, laminin, and the heparan sulfate proteoglycan termed perlecan). Although the distribution and origin of both collagen IV and laminin have been well documented in the liver, perlecan has been poorly investigated, so far. We have studied the distribution and cellular origin of perlecan in rat livers in various conditions as well as in hepatocyte primary culture. By immunolocalization in both adult and 18-day-old fetal liver, perlecan was found in portal spaces, around central veins, and throughout the lobule. Immunoelectron microscopy revealed its presence at the level of basement membranes surrounding bile ducts and blood vessels, and in the space of Disse discontinuously interacting with hepatocyte microvilli. Precursors of perlecan were detected in the rough endoplasmic reticulum of bile duct cells and both vascular and sinusoidal endothelial cells. Both hepatocytes and Ito cells were negative. Northern-blot analysis confirmed the lack of appreciable expression of perlecan in hepatocytes isolated from either fetal or adult livers. In 18-month-diethylnitrosamine-treated rat liver, perlecan was abundant in neoplastic nodules. Electron microscopic investigation revealed an almost continuous layer of perlecan in the space of Disse and intracellular staining in sinusoidal endothelial cells, only. Perlecan mRNAs were detectable in malignant nodules, and absent in hepatocytes from nontumorous areas. Hepatocytes expressed high levels of perlecan mRNAs only when put in culture. This expression was reduced in conditions that allow improvement of hepatocyte survival and function (ie addition of corticoids, dimethylsulfoxide or nicotinamide to the medium, or in coculture with liver epithelial cells from biliary origin). Immunolocalization by light and electron microscopy showed that deposition of the proteoglycan occurred in coculture, in basement membranelike structures located around hepatocyte cords. In vitro attachment assay of hepatocytes on purified perlecan substrate indicated that these cells may interact with the proteoglycan through integrins which belong to the beta 1 family. These data suggest that deposition of perlecan in the space of Disse requires cellular cooperation. This article on perlecan, the third major component of hepatic basement membranes, shows a unique cellular origin in the liver and, as found for both collagen IV and laminin, an expression in adult hepatocytes when place in culture.
机译:基底膜包含三个主要成分(即胶原IV,层粘连蛋白和硫酸乙酰肝素蛋白聚糖,称为Perlecan)。尽管胶原IV和层粘连蛋白在肝脏中的分布和来源均已得到充分证明,但到目前为止,人们对Perlecan的研究还很少。我们已经研究了在不同条件下以及在肝细胞原代培养中大鼠肝中白勒胶的分布和细胞起源。通过在成年和18日龄胎儿肝脏中进行免疫定位,在门脉空间,中心静脉周围以及整个小叶中发现了珍珠岩。免疫电子显微镜检查显示其存在于胆管和血管周围的基底膜水平,并且在Disse的空间中不连续地与肝细胞微绒毛相互作用。在胆管细胞的粗糙内质网以及血管和正弦血管内皮细胞中均检测到perlecan的前体。肝细胞和伊藤细胞均为阴性。 Northern印迹分析证实,从胎儿或成年肝脏分离的肝细胞中,perlecan表达不足。在用18个月的二乙基亚硝胺治疗的大鼠肝脏中,珍珠岩富含肿瘤性结节。电子显微镜研究仅在Disse的空间中发现了一层几乎连续的珍珠层,而在窦状内皮细胞中则只有细胞内染色。 Perlecan mRNA在恶性结节中可检测到,而在非肿瘤区域的肝细胞中则不存在。肝细胞仅在培养时才表达高水平的珍珠油mRNA。在允许改善肝细胞存活和功能的条件下(即向培养基中添加皮质类固醇,二甲基亚砜或烟酰胺,或与胆源性肝上皮细胞共培养),该表达降低。通过光学和电子显微镜的免疫定位表明,蛋白聚糖的沉积在共培养中发生在位于肝细胞索周围的基底膜样结构中。肝细胞在纯化的Perlecan底物上的体外附着测定表明,这些细胞可能通过属于β1家族的整联蛋白与蛋白聚糖相互作用。这些数据表明,Perlecan在Disse空间中的沉积需要细胞合作。这篇关于全珠蛋白(肝基底膜的第三个主要成分)的文章显示了肝脏中独特的细胞起源,并且就胶原IV和层粘连蛋白而言,在培养时在成年肝细胞中都有表达。

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